FDA Inspection 963563 - Oscor Inc. - March 17, 2016

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Record Details

This FDA Inspection record concerns Oscor Inc., with an inspection on March 17, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Oscor Inc.
Inspection Date: March 17, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 59526ba3-2c72-467c-95fd-262f46388dae

Violation Codes10

21 CFR 803.50(a)(1)21 CFR 803.50(a)(2)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.30(f)21 CFR 820.5021 CFR 820.70(a)

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